chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62108979221089793G28GENIChomozygous134421664
62108980521089806T26GENIChomozygous134421665
62108980821089809C25GENIChomozygous134421666
62108981221089814CC25GENIChomozygous134421667
62108981521089816T25GENIChomozygous134421668
62108982821089829AC24GENIChomozygous114735297
62108983921089840C23GENIChomozygous134421669
62108985821089859AC19GENIChomozygous114735299
62108986321089866CTA18GENIChomozygous134421670
62108987321089874G17GENIChomozygous134421671
62108988021089881C13GENIChomozygous134421672
62108988721089889TA10GENIChomozygous134421673
62108989221089893A9GENIChomozygous134421674
62108990021089901C9GENIChomozygous134421675
62108990321089904C8GENIChomozygous134421676
62108990821089909C8GENIChomozygous134421677
62108991721089918A5GENIChomozygous134421678
62108992221089924GG2GENIChomozygous134421679
62108992821089940GGAGGTGAGGAG2GENIChomozygous134421680
62108995621089956G1GENIChomozygous134421681
62108996221089963C1GENIChomozygous134421682
62108996521089966CA1GENIChomozygous134423737
62108997421089974GAGAGAGAGAG1GENIChomozygous134421683
62108998621089988GC3GENIChomozygous134421684
62108999021089991C3GENIChomozygous134421685
62116986621169867GC16GENIChomozygous115050514